Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Valérie Buée-Scherrer"'
Autor:
Isabel Paiva, Lucrezia Cellai, Céline Meriaux, Lauranne Poncelet, Ouada Nebie, Jean-Michel Saliou, Anne-Sophie Lacoste, Anthony Papegaey, Hervé Drobecq, Stéphanie Le Gras, Marion Schneider, Enas M. Malik, Christa E. Müller, Emilie Faivre, Kevin Carvalho, Victoria Gomez-Murcia, Didier Vieau, Bryan Thiroux, Sabiha Eddarkaoui, Thibaud Lebouvier, Estelle Schueller, Laura Tzeplaeff, Iris Grgurina, Jonathan Seguin, Jonathan Stauber, Luisa V. Lopes, Luc Buée, Valérie Buée-Scherrer, Rodrigo A. Cunha, Rima Ait-Belkacem, Nicolas Sergeant, Jean-Sébastien Annicotte, Anne-Laurence Boutillier, David Blum
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 12 (2022)
Caffeine is the most widely consumed psychoactive substance in the world. Strikingly, the molecular pathways engaged by its regular consumption remain unclear. We herein addressed the mechanisms associated with habitual (chronic) caffeine consumption
Externí odkaz:
https://doaj.org/article/180844816fc24e34ba8881f1763587a8
Autor:
Hamza Benderradji, Sarra Kraiem, Emilie Courty, Sabiha Eddarkaoui, Cyril Bourouh, Emilie Faivre, Laure Rolland, Emilie Caron, Mélanie Besegher, Frederik Oger, Theo Boschetti, Kévin Carvalho, Bryan Thiroux, Thibaut Gauvrit, Emilie Nicolas, Victoria Gomez-Murcia, Anna Bogdanova, Antonino Bongiovanni, Anne Muhr-Tailleux, Steve Lancel, Kadiombo Bantubungi, Nicolas Sergeant, Jean-Sebastien Annicotte, Luc Buée, Didier Vieau, David Blum, Valérie Buée-Scherrer
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Alzheimer’s disease (AD) is the leading cause of dementia. While impaired glucose homeostasis has been shown to increase AD risk and pathological loss of tau function, the latter has been suggested to contribute to the emergence of the glucose home
Externí odkaz:
https://doaj.org/article/67b740be6a384290b9ac72a4124826f9
Autor:
Nicolas Sergeant, Valérie Vingtdeux, Sabiha Eddarkaoui, Marion Gay, Caroline Evrard, Nicolas Le Fur, Cyril Laurent, Raphaelle Caillierez, Hélène Obriot, Paul-Emmanuel Larchanché, Amaury Farce, Mathilde Coevoet, Pascal Carato, Mostafa Kouach, Amandine Descat, Patrick Dallemagne, Valérie Buée-Scherrer, David Blum, Malika Hamdane, Luc Buée, Patricia Melnyk
Publikováno v:
Neurobiology of Disease, Vol 129, Iss , Pp 217-233 (2019)
Alzheimer's Disease is a devastating dementing disease involving amyloid deposits, neurofibrillary tangles, progressive and irreversible cognitive impairment. Today, only symptomatic drugs are available and therapeutic treatments, possibly acting at
Externí odkaz:
https://doaj.org/article/81981f930cdb439bb251f4f9165c75b8
Autor:
Julie Cazareth, Raphaëlle Pardossi-Piquard, Arnaud Mary, Inger Lauritzen, Renaud Bussiere, Alexandre Bourgeois, Véronique Paquis-Flucklinger, Sandra Lacas-Gervais, Paula Fernanda Kinoshita, Konstantina Fragaki, Frédéric Checler, Loan Vaillant-Beuchot, Rosanna Mary, Mounia Chami, Valérie Buée-Scherrer, Sophie Pagnotta, Cécile Martin, Fanny Eysert, Charlotte Bauer, Céline Badot, Luc Buée
Publikováno v:
Acta Neuropathologica
Acta Neuropathologica, Springer Verlag, 2020, ⟨10.1007/s00401-020-02234-7⟩
Acta Neuropathologica, Springer Verlag, 2020, ⟨10.1007/s00401-020-02234-7⟩
Several lines of recent evidence indicate that the amyloid precursor protein-derived C-terminal fragments (APP-CTFs) could correspond to an etiological trigger of Alzheimer’s disease (AD) pathology. Altered mitochondrial homeostasis is considered a
Autor:
Audrey Hector, Christina McAnulty, Maude-Eloise Piche-Lemieux, Jonathan Brouillette, Claire Alves-Pires, Valérie Buée-Scherrer, Luc Buée
Publikováno v:
FASEB Journal
FASEB Journal, 2020, 34 (2), pp.2968-2977. ⟨10.1096/fj.201902135R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2020, 34 (2), pp.2968-2977. ⟨10.1096/fj.201902135R⟩
FASEB Journal, 2020, 34 (2), pp.2968-2977. ⟨10.1096/fj.201902135R⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2020, 34 (2), pp.2968-2977. ⟨10.1096/fj.201902135R⟩
International audience; Tau hyperphosphorylation is a major neuropathological hallmark of many neurodegenerative disorders such as Alzheimer's disease. Several anesthetics have been shown previously to induced marked tau hyperphosphorylation. Althoug
Autor:
Christina McAnulty, Valérie Buée-Scherrer, Jonathan Brouillette, Maude-Eloise Piche-Lemieux, Luc Buée, Audrey Hector, Claire Alves-Pires
Publikováno v:
Alzheimer's & Dementia. 16
Publikováno v:
Data in Brief
Data in Brief, Elsevier, 2020, 31, pp.105921. ⟨10.1016/j.dib.2020.105921⟩
Data in Brief, 2020, 31, pp.105921. ⟨10.1016/j.dib.2020.105921⟩
Data in Brief, Vol 31, Iss, Pp 105921-(2020)
Data in Brief, Elsevier, 2020, 31, pp.105921. ⟨10.1016/j.dib.2020.105921⟩
Data in Brief, 2020, 31, pp.105921. ⟨10.1016/j.dib.2020.105921⟩
Data in Brief, Vol 31, Iss, Pp 105921-(2020)
International audience; The data presented in this paper are related to the research article "Functional characterization of a FUS mutant zebrafish line as a novel genetic model for ALS". In this model the lack of fus causes reduced lifespan as well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8df691caf39674ca1b2a0a3c95e548c0
https://hal.sorbonne-universite.fr/hal-02934553
https://hal.sorbonne-universite.fr/hal-02934553
Autor:
Francisco, Fernandez-Gomez, Helene, Tran, Claire-Marie, Dhaenens, Marie-Laure, Caillet-Boudin, Susanna, Schraen-Maschke, David, Blum, Bernard, Sablonnière, Valérie, Buée-Scherrer, Luc, Buee, Nicolas, Sergeant
Publikováno v:
Advances in experimental medicine and biology. 1184
Myotonic dystrophies (DM) are rare inherited neuromuscular disorders linked to microsatellite unstable expansions in non-coding regions of ubiquitously expressed genes. The DMPK and ZNF9/CNBP genes which mutations are responsible for DM1 and DM2 resp
Publikováno v:
Neurobiology of Disease, Vol 142, Iss, Pp 104935-(2020)
Mutations in Fused in sarcoma (FUS), an RNA-binding protein, are known to cause Amyotrophic Lateral Sclerosis (ALS). However, molecular mechanisms due to loss of FUS function remain unclear and controversial. Here, we report the characterization and
Autor:
Susanna Schraen-Maschke, Nicolas Sergeant, Helene Tran, Marie-Laure Caillet-Boudin, Bernard Sablonnière, David Blum, Claire-Marie Dhaenens, Luc Buée, Valérie Buée-Scherrer, Francisco J. Fernandez-Gomez
Publikováno v:
Tau Biology
Tau Biology, pp.207-216, 2019, ⟨10.1007/978-981-32-9358-8_17⟩
Advances in Experimental Medicine and Biology ISBN: 9789813293571
Tau Biology, pp.207-216, 2019, ⟨10.1007/978-981-32-9358-8_17⟩
Advances in Experimental Medicine and Biology ISBN: 9789813293571
Myotonic dystrophies (DM) are rare inherited neuromuscular disorders linked to microsatellite unstable expansions in non-coding regions of ubiquitously expressed genes. The DMPK and ZNF9/CNBP genes which mutations are responsible for DM1 and DM2 resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ccb09502dd8ef54cdfcca367d093887
https://hal.archives-ouvertes.fr/hal-02541222
https://hal.archives-ouvertes.fr/hal-02541222